2 research outputs found
A Triangular Platinum(II) Multi-nuclear Complex with Impressive Cytotoxicity Towards Breast Cancer Stem Cells.
The preparation of multi-nuclear metal complexes offers a route to novel anticancer agents and delivery systems. The potency of a novel triangular multi-nuclear complex containing three platinum atoms, Pt-3, towards breast cancer stem cells (CSCs) is reported. The tri-nuclear platinum(II) complex, Pt-3 exhibits selectivity toxicity towards breast CSCs over bulk breast cancer cells and non-tumorigenic breast cells. Remarkably, Pt-3 inhibits the formation, size, and viability of mammospheres to a better extent than salinomycin, an established CSC-potent agent, and cisplatin and carboplatin, clinically used platinum drugs. Mechanism of action studies show that Pt-3 effectively enters breast CSCs, penetrates the nucleus, induces genomic DNA damage, and prompts caspase-dependent apoptosis. To the best of our knowledge, Pt-3 is the first multi-nuclear platinum complex to selectivity kill breast CSCs over other breast cell types
Temperature-Dependent Semiconducting Behavior of an Organic Cocrystal Driven by the Stacking Mode of Interaction of a 4,4′-Bipyridine Molecule
Organic cocrystals based on H-bonding as well as π-stacking
interactions between 4,4′-bipyridine–pyromellitic acid
(1) and 4,4′-bipyridine–phthalic acid (2) are reported. Cocrystals 1 and 2 were fully characterized by single-crystal X-ray diffraction and
NMR and IR spectroscopy. The single-crystal X-ray diffraction shows
the H stacking pattern of the adjacent 4,4′-bipyridine molecules
in the construction of a 3D chain structure for cocrystal 1. Cocrystal 2, however, formed a zigzag 3D chain where
the adjacent 4,4′-bipyridyl molecules are involved in a J-stacking
mode. Experimental conductivity measurements of the cocrystals 1 and 2 with a Keithley 4200 SCS parameter analyzer
showed the temperature-dependent semiconducting behavior in the case
of cocrystal 1, whereas cocrystal 2 remained
as an insulator. The favorable H-stacking interaction of 4,4′-bipyridine
molecules which is the prime origin of semiconductivity in cocrystal 1 may become out of phase due to the free rotation along the
C–C bond of 4,4′-bipyridine with an increase in temperature.
Although the semiconducting behavior of a material increases with
increasing temperature and decreases in resistivity, in the case of
cocrystal 1 due to the probable phase transition of the
4,4′-bipyridyl molecules the material became an insulator with
an increase in temperature from 20 °C to higher temperature,
whereas the semiconducting behavior was restored after cooling the
crystals to 20 °C again. The theoretical study conducted with
the optimized structures of 1 and 2 showed
the higher electron hopping rate in the case of cocrystal 1 as compared to 2 which can account for the charge conduction
in the case of 1